• Cochrane Db Syst Rev · Apr 2009

    Review

    Huperzine A for vascular dementia.

    • Zilong Hao, Ming Liu, Zhiqin Liu, and Donghao Lv.
    • Department of Neurology, West China Hospital, Sichuan University, No. 37, Guo Xue Xiang, Chengdu, Sichuan Province, China, 610041.
    • Cochrane Db Syst Rev. 2009 Apr 15 (2): CD007365CD007365.

    BackgroundHuperzine A, a form of herbal medicine, has been considered as an alternative treatment for vascular dementia (VaD) in China.ObjectivesTo assess the efficacy and safety of Huperzine A in patients with vascular dementia.Search StrategyThe Specialized Register of the Cochrane Dementia and Cognitive Improvement Group (CDCIG) was searched on 7 July 2008 using the terms: huperzi* OR ayapin OR scoparon*. The CDCIG Specialized Register contains records from all major health care databases (The Cochrane Library, MEDLINE, EMBASE, PsycINFO, CINAHL, LILACS) as well as from many trials databases and grey literature sources. The review authors searched the following databases in August 2008 using the terms 'Huperzine A', 'Shishanjianjia', 'Haboyin' and 'Shuangyiping': The Chinese Biomedical Database (CBM) (1977 to August 2008); Chinese Science and Technique Journals Database (VIP) (1989 to August 2008); China National Knowledge Infrastructure (CNKI) (1979 to August 2008); The Chinese Clinical Trials Register (ChiCTR, August 2008); Google (August 2008). In addition, the review authors searched reference lists, relevant clinical trials and contacted researchers in an effort to identify further published and unpublished studies.Selection CriteriaRandomized controlled trials comparing Huperzine A with placebo in patients with vascular dementia were considered eligible for inclusion.Data Collection And AnalysisTwo review authors independently selected trials for inclusion, assessed trial quality, and extracted data.Main ResultsOnly one small trial, involving 14 participants, was included. No significant beneficial effect of Huperzine A on the improvement of cognitive function measured by MMSE for VaD (WMD 2.40; 95% CI -4.78 to 9.58) was observed. No death from all causes at the end of treatment were reported. At present, other outcome measures were not available in any of the trials. Although no statistically significant differences were found between the Huperzine A-treated and control groups, the confidence intervals for the treatment effect estimates were wide and included both clinically significant benefits and clinically significant harms.Authors' ConclusionsThere is no [convincing] evidence that Huperzine A is of value in vascular dementia based on one small trial. It deserves further research.

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